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dc.contributor.authorTansini, Paula Baldisserapt_BR
dc.contributor.authorBoff, Ana Letíciapt_BR
dc.contributor.authorWeber, Magda Blessmannpt_BR
dc.contributor.authorBonamigo, Renan Rangelpt_BR
dc.date.accessioned2020-07-23T03:40:33Zpt_BR
dc.date.issued2020pt_BR
dc.identifier.issn0365-0596pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/212341pt_BR
dc.description.abstractHailey-Hailey disease, or familial benign pemphigus, is a rare bullous genodermatosis that usually presents with flaccid blisters, erosions, and maceration limited to flexural areas, resulting in increased morbidity and reduced quality of life for affected patients. The authors report an unusual case of generalized Hailey-Hailey disease with erythroderma and fatal outcome.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofAnais brasileiros de dermatologia. Vol. 95, no. 1 (2020), p. 75-77pt_BR
dc.rightsOpen Accessen
dc.subjectPênfigo familiar benignopt_BR
dc.subjectPemphigus, benign familialen
dc.subjectDermatitis, exfoliativeen
dc.subjectDermatite esfoliativapt_BR
dc.subjectSkin diseasesen
dc.subjectRelatos de casospt_BR
dc.subjectVesiculobullousen
dc.titleFamilial ‘‘benign’’ pemphigus? Erythroderma and fatal outcomept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001114856pt_BR
dc.type.originNacionalpt_BR


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